To Evaluate the effect of mustadi yapana basti on the process of spermatogenesis

Not Applicable

Completed

• Conditions: Health Condition 1: N461- Oligospermia

• Registration Number: CTRI/2019/08/020538
• Lead Sponsor: AYURVEDIC AND UNANI TIBBIA COLLEGE

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-03-21
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 32

Inclusion Criteria

2.No history of serious illness or disease

3.Not under any type of medical treatment since last six months.

4.Subjects having sperm count 05 to 15 million per ml (Group A)

5.Subjects having sperm count More than 15 million per ml (Group B).

6.Subjects who are able to come for follow up on fixed visits and are well aware about the treatment plans.

7.Subjects willing to participate and able to give written informed consent

Exclusion Criteria

1.Subject having Age below 20 years and more than 40 year

2.Patients suffering from congenital anomalies

3.Subject of Type-I DM or Type-II DM on insulin

4.Hereditary Disease

5.The patients having Varicocele, Testicular maldescent, previous reproductive surgery, STD were excluded

6.Patient of Azoospermia and Aspermia.

7.Taking treatment for major psychiatric problem.

8.Illness necessitating long term drug treatment (Rheumatoid arthritis ,Diabetes Mellitus ,Psychoneuro endocrinal disorder ,TB,AIDS)

9.Uncontrolled Hypertensive patients (BP with or without medication greater than 140/90mm Hg after 5 min of rest)

10.Subjects with any unstable heart disease or known case of MI ,Unstable angina.

11.Subjects who have a recent history or who are currently known to abuse of alcohol or drugs.

12.Subjects on systemic or oral steroids.

13.H/o hypersensitivity to any of the Herbs to be use in intervention.

14.Subjects who have completed participation in any other clinical trial during the past six month.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
EFFECT ON SPERM COUNT AND BIOMARKERS OF SPERMATOGENESISTimepoint: ONE MONTH

Secondary Outcome Measures

Name	Time	Method
IMPROVEMENT ON INTERNATIONAL ERECTILE DYSFUNCTION SCORE AND LAKSHAN OF SHUKRA KSHYATimepoint: ONE MONTH